Adenylyl cyclase 3 regulates osteocyte mechanotransduction and primary cilium

• Published in: Biochemical and biophysical research communications 2021-10, Vol.573, p.145-150
• Main Authors: Duffy, Michael P., Sup, McKenzie E., Guo, X. Edward
• Format: Article
• Language: English
• Subjects: Adenylyl cyclase 3; cAMP; Gsk3beta; Mechanotransduction; Osteocyte; Primary cilium
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2021.08.033

Osteocytes are accepted as the primary mechanosensing cell in bone, but how they translate mechanical signals into biochemical signals remains unclear. Adenylyl cyclases (AC) are enzymes that catalyze the production of second messenger cyclic adenosine monophosphate (cAMP). Osteocytes display a biphasic, cAMP response to fluid shear with an initial decrease in cAMP concentrations and then an increased concentration after sustained mechanical stimulation. To date, AC6, a calcium-inhibited AC, is the primary isoform studied in bone. Since osteocytes are calcium-responsive mechanosensors, we asked if a calcium-stimulated isoform contributes to mechanotransduction. Using a transcriptomic dataset of MLO-Y4 osteocyte-like cells from the NIH Gene Expression Omnibus, we identified AC3 as the only calcium-stimulated isoform expressed. We show that inhibiting AC3 in MLO-Y4 cells results in decreased cAMP-signaling with fluid shear and increased osteogenic response to fluid flow (measured as Ptgs2 expression) of longer durations, but not shorter. AC3 likely contributes to osteocyte mechanotransduction through a signaling axis involving the primary cilium and GSK3β. We demonstrate that AC3 localizes to the primary cilium, as well as throughout the cytosol and that fluid-flow regulation of primary cilia length is altered with an AC3 knockdown. Regulation of GSK3β is downstream of the primary cilium and cAMP signaling, and with western blots we found that GSK3β inhibition by phosphorylation is increased after fluid shear in AC3 knockdown groups. Our data show that AC3 contributes to osteocyte mechanotransduction and warrants further investigation to pave the way to identifying new therapeutic targets to treat bone disease like osteoporosis. •AC3 is the only calcium-stimulated adenylyl cyclase isoform osteocytes express.•Inhibition of AC3 leads to untampered osteocyte mechanoresponse.•Inhibition of AC3 reduces cAMP production in response to fluid shear.•AC3 localizes to the primary cilium in vitro and in vivo.•AC3 contributes to fluid shear regulation of primary cilia and GSK3beta.